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Cenicriviroc in mild liver impaired

Tobira Therapeutics, Inc. · Phase 1 active Small molecule Quality 45/100

Cenicriviroc in mild liver impaired is a CCR2/CCR5 dual antagonist Small molecule drug developed by Tobira Therapeutics, Inc.. It is currently in Phase 1 development. Also known as: CVC.

Cenicriviroc blocks CCR2 and CCR5 chemokine receptors, inhibiting inflammatory cell recruitment and fibrosis progression in liver disease.

Likelihood of approval
9.6% vs 9.6% industry baseline
If approved by FDA: likely 2033–2036
Steps remaining: Phase 2 → Phase 3 → NDA/BLA submission
Confidence: Medium
Why this estimate
  • Baseline phase 1 → approval rate +9.6pp
    Industry-wide phase 1 drugs reach approval ~9.6% of the time (BIO/Informa 2023 industry benchmark across all therapeutic areas).
Predicted approval windows by jurisdiction (conditional on FDA approval)
Regulator Country Likely year Lag vs FDA
FDA US 2033–2036
EMA EU 2034–2037 +0.7 yr
MHRA GB 2034–2037 +0.7 yr
Health Canada CA 2034–2038 +0.9 yr
TGA AU 2034–2038 +1.2 yr
PMDA JP 2034–2038 +1.5 yr
NMPA CN 2035–2039 +2.3 yr
MFDS KR 2034–2038 +1.4 yr
CDSCO IN 2034–2039 +1.8 yr
ANVISA BR 2035–2039 +2.3 yr

Hover any row for the lag rationale. Lag estimates are reduced when the drug has FDA Breakthrough or EMA PRIME designation (sponsors file globally in parallel).

Estimate based on the BIO/Informa industry phase transition rates plus per-drug modifiers for therapeutic area, sponsor type, FDA designations, mechanism, and trial design. Per-jurisdiction lags from Tufts CSDD international approval studies. Not investment, clinical or regulatory advice. Methodology: /methodology#likelihood.

At a glance

Generic nameCenicriviroc in mild liver impaired
Also known asCVC
SponsorTobira Therapeutics, Inc.
Drug classCCR2/CCR5 dual antagonist
ModalitySmall molecule
PhasePhase 1

Mechanism of action

By antagonizing CCR2, cenicriviroc reduces monocyte and macrophage infiltration that drives hepatic inflammation and fibrosis. CCR5 blockade provides additional anti-inflammatory effects. This dual mechanism targets key pathways in chronic liver disease progression.

Approved indications

Common side effects

No common side effects on file.

Key clinical trials

Primary sources

Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.

SourceUsed for
ClinicalTrials.govTrial enrolment, design, endpoints, results

Competitive intelligence

For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape:

Frequently asked questions about Cenicriviroc in mild liver impaired

What is Cenicriviroc in mild liver impaired?

Cenicriviroc in mild liver impaired is a CCR2/CCR5 dual antagonist drug developed by Tobira Therapeutics, Inc..

How does Cenicriviroc in mild liver impaired work?

Cenicriviroc blocks CCR2 and CCR5 chemokine receptors, inhibiting inflammatory cell recruitment and fibrosis progression in liver disease.

Who makes Cenicriviroc in mild liver impaired?

Cenicriviroc in mild liver impaired is developed by Tobira Therapeutics, Inc. (see full Tobira Therapeutics, Inc. pipeline at /company/tobira-therapeutics-inc).

Is Cenicriviroc in mild liver impaired also known as anything else?

Cenicriviroc in mild liver impaired is also known as CVC.

What drug class is Cenicriviroc in mild liver impaired in?

Cenicriviroc in mild liver impaired belongs to the CCR2/CCR5 dual antagonist class. See all CCR2/CCR5 dual antagonist drugs at /class/ccr2-ccr5-dual-antagonist.

What development phase is Cenicriviroc in mild liver impaired in?

Cenicriviroc in mild liver impaired is in Phase 1.

Related

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing